Massachusetts General Hospital Cancer Center and Department of Medicine, Harvard Medical School, 13(th) Street, Charlestown, MA 02129, USA.
Mol Cell. 2012 Nov 30;48(4):491-507. doi: 10.1016/j.molcel.2012.11.006.
Histone lysine methylation has emerged as a critical player in the regulation of gene expression, cell cycle, genome stability, and nuclear architecture. Over the past decade, a tremendous amount of progress has led to the characterization of methyl modifications and the lysine methyltransferases (KMTs) and lysine demethylases (KDMs) that regulate them. Here, we review the discovery and characterization of the KMTs and KDMs and the methyl modifications they regulate. We discuss the localization of the KMTs and KDMs as well as the distribution of lysine methylation throughout the genome. We highlight how these data have shaped our view of lysine methylation as a key determinant of complex chromatin states. Finally, we discuss the regulation of KMTs and KDMs by proteasomal degradation, posttranscriptional mechanisms, and metabolic status. We propose key questions for the field and highlight areas that we predict will yield exciting discoveries in the years to come.
组蛋白赖氨酸甲基化已成为调节基因表达、细胞周期、基因组稳定性和核结构的关键因素。在过去的十年中,大量的研究进展使得甲基化修饰以及调控它们的赖氨酸甲基转移酶(KMTs)和赖氨酸去甲基化酶(KDMs)得以被描绘出来。在这里,我们回顾了 KMTs 和 KDMs 的发现和特性,以及它们调控的甲基化修饰。我们讨论了 KMTs 和 KDMs 的定位以及赖氨酸甲基化在整个基因组中的分布。我们强调了这些数据如何使我们将赖氨酸甲基化视为复杂染色质状态的关键决定因素。最后,我们讨论了 KMTs 和 KDMs 的调节,包括蛋白酶体降解、转录后机制和代谢状态。我们为该领域提出了关键问题,并强调了我们预测在未来几年将产生令人兴奋发现的领域。